Xueya Zhou

发表

Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians

Tien Yin Wong, Wei Huang, Takao Sugiyama, 2011, Nature Genetics.

Dissecting Autism Genetic Risk Using Single-cell RNA-seq Data

Yufeng Shen, Xueya Zhou, Siying Chen, 2020, bioRxiv.

Exome sequencing of 457 autism families recruited online provides evidence for novel ASD genes

Richard A Marini, Simon X. Xu, Nicole M. Russo-Ponsaran, 2019 .

Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes

Richard A Marini, Simon X. Xu, Deana D. Li, 2019, npj Genomic Medicine.

Integrated analysis of mRNA-seq and miRNA-seq for host susceptibilities to influenza A (H7N9) infection in inbred mouse lines

You-Qiang Song, K. Yuen, Xueya Zhou, 2018, Functional & Integrative Genomics.

Identification of long non-protein coding RNAs in chicken skeletal muscle using next generation sequencing.

Tingting Li, Dahai Zhu, Xueya Zhou, 2012, Genomics.

Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation

Jing He, Christian Gieger, Wei Huang, 2015, Nature Genetics.

Title Polygenic scores using summary statistics via penalized regression Author list

P. Sham, Xueya Zhou, S. Choi, 2016 .

Trans-Ethnic Polygenic Analysis Supports Genetic Overlaps of Lumbar Disc Degeneration With Height, Body Mass Index, and Bone Mineral Density

P. Sham, You-Qiang Song, Y. Hsu, 2018, bioRxiv.

Identification and characterization of human snoRNA core promoters.

Tingting Li, Dahai Zhu, Xueya Zhou, 2010, Genomics.

Prioritizing genes responsible for host resistance to influenza using network approaches

Xuegong Zhang, You-Qiang Song, K. To, 2013, BMC Genomics.

Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH

W. Chung, Yufeng Shen, Yicheng Guo, 2020, bioRxiv.

Exome Sequencing and Gene Prioritization Correct Misdiagnosis in a Chinese Kindred with Familial Amyloid Polyneuropathy

Xuegong Zhang, P. Sham, H. Chen, 2016, Scientific Reports.

Mutations in Hnrnpa1 cause congenital heart defects

P. Sham, P. Kwok, You-Qiang Song, 2018, JCI insight.

Mutations in Hnrnpa 1 cause congenital heart defects

P. Sham, P. Kwok, You-Qiang Song, 2018 .

Title Mutations in Hnrnpa 1 cause congenital heart defects

P. Sham, P. Kwok, You-Qiang Song, 2018 .

De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders

W. Chung, Yufeng Shen, P. Donahoe, 2018, PLoS genetics.

Psychiatric and Medical Profiles of Autistic Adults in the SPARK Cohort

Richard A Marini, Simon X. Xu, Nicole M. Russo-Ponsaran, 2020, Journal of Autism and Developmental Disorders.

Common variants in the ATP2B1 gene are associated with hypertension and arterial stiffness in Chinese population

Xueya Zhou, Dingliang Zhu, P. Gao, 2012, Molecular Biology Reports.

Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

Richard A Marini, W. T. Harvey, Bradley P. Coe, 2020, Nature Communications.

A Rare Variant at the KYNU Gene Is Associated With Kynureninase Activity and Essential Hypertension in the Han Chinese Population

X. Jeunemaître, Xueya Zhou, Dingliang Zhu, 2011, Circulation. Cardiovascular genetics.

Xuegong Zhang, Xueya Zhou, Ying'ai Zhang, 2014, Acta Haematologica.

Integrating de novo and inherited variants in over 42,607 autism cases identifies mutations in new moderate risk genes

William T. Harvey, Richard A Marini, Simon X. Xu, 2021, medRxiv.

Rare and de novo variants in 827 congenital diaphragmatic hernia probands implicate LONP1 as candidate risk gene.

W. Chung, Yufeng Shen, P. Donahoe, 2021, American journal of human genetics.

Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes

B. O’Roak, E. Eichler, W. Chung, 2019, npj Genomic Medicine.

Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes

Richard A Marini, Simon X. Xu, Nicole M. Russo-Ponsaran, 2019, npj Genomic Medicine.

Polygenic scores via penalized regression on summary statistics

Pak Chung Sham, Timothy Shin Heng Mak, Robert Milan Porsch, 2016, bioRxiv.

CNV analysis in Chinese children of mental retardation highlights a sex differentiation in parental contribution to de novo and inherited mutational burdens

Xuegong Zhang, P. Sham, Xueya Zhou, 2016, Scientific Reports.

A dominant negative mutation at the ATP binding domain of AMHR2 is associated with a defective anti-Müllerian hormone signaling pathway.

Wei Zhang, Xueya Zhou, Binbin Wang, 2016, Molecular human reproduction.

Co-occurring protein phosphorylation are functionally associated

Ying Li, Tingting Li, Xueya Zhou, 2017, PLoS Comput. Biol..

Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index.

Y. J. Kim, D. Absher, T. Assimes, 2014, Human molecular genetics.

Polymorphisms at 16p13 are associated with systemic lupus erythematosus in the Chinese population

Liangdan Sun, Xuejun Zhang, Jian-Wen Han, 2010, Journal of Medical Genetics.

Exome Sequencing Identifies a Novel Frameshift Mutation of MYO6 as the Cause of Autosomal Dominant Nonsyndromic Hearing Loss in a Chinese Family

Xuegong Zhang, P. Sham, J. Chen, 2014, Annals of human genetics.

Resolving the genetic heterogeneity of prelingual hearing loss within one family: Performance comparison and application of two targeted next generation sequencing approaches

Xuegong Zhang, K. Choy, Xueya Zhou, 2014, Journal of Human Genetics.

Systematic Characterization and Prediction of Post-Translational Modification Cross-Talk*

Rui Jiang, Ying Li, Xueya Zhou, 2015, Molecular & Cellular Proteomics.

Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

Richard A Marini, W. T. Harvey, B. Coe, 2020, Nature Communications.

Polygenic scores using summary statistics via penalized regression

Robert Milan Porsch, Shing Wan Choi, Xueya Zhou, 2016 .

Rare Variant at the KYNU Gene is Associated with Kynureninase Activity and Essential Hypertension in the Han Chinese Population Running title :

X. Jeunemaître, Xueya Zhou, Dingliang Zhu, 2011 .

Likely damaging de novo variants in congenital diaphragmatic hernia patients are associated with worse clinical outcomes

W. Chung, Yufeng Shen, D. Potoka, 2020, Genetics in Medicine.

Identification and functional analysis of a novel LHX1 mutation associated with congenital absence of the uterus and vagina

Xuegong Zhang, Xueya Zhou, Binbin Wang, 2017, Oncotarget.

A rare variant in MLKL confers susceptibility to ApoE ɛ4-negative Alzheimer's disease in Hong Kong Chinese population

You-Qiang Song, Jiang-Man Li, H. Mak, 2018, Neurobiology of Aging.

Beliefs in vaccine as causes of autism among SPARK cohort caregivers.

Richard A Marini, Simon X. Xu, Jacob B. Hall, 2020, Vaccine.

Likely damaging de novo variants in congenital diaphragmatic hernia patients are associated with worse clinical outcomes

Yufeng Shen, D. Chung, D. Potoka, 2020, Genetics in Medicine.

Genetic analysis of de novo variants reveals sex differences in complex and isolated congenital diaphragmatic hernia and indicates MYRF as a candidate gene

W. Chung, D. Nickerson, Yufeng Shen, 2017, bioRxiv.

Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations.

Xiaofeng Zhu, Todd L Edwards, Wei Guo, 2013, American journal of human genetics.

Common variants in the ATP2B1 gene are associated with hypertension and arterial stiffness in Chinese population

Xuegong Zhang, Xueya Zhou, Dingliang Zhu, 2013, Molecular Biology Reports.

Short read mapping for exome sequencing.

Xuegong Zhang, Binbin Wang, You-Qiang Song, 2013, Methods in molecular biology.

Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations.

Andrew D. Johnson, Jeanette S. Andrews, M. Fornage, 2013, American journal of human genetics.

A novel non-synonymous mutation in the homeodomain of HOXD13 causes synpolydactyly in a Chinese family.

Xueya Zhou, Binbin Wang, Longfei Cheng, 2012, Clinica chimica acta; international journal of clinical chemistry.

Polymorphisms at 16p13 are associated with systemic lupus erythematosus in the Chinese population

Liangdan Sun, Xuejun Zhang, Jian-Wen Han, 2010, Journal of Medical Genetics.